Efficient Synthesis of 2′-Bromo-2′-Deoxy-3′,5′-O-TPDS-pyrimidine Nucleosides by Boron Trifluoride Catalyzed Reaction of O2,2′-Anhydro-(1-β-D-Arabinofuran0Syl)pyrimidine Nucleosides with Lithium Bromide
Author:
Affiliation:
1. a Laboratory of Pharmaceutical Chemistry, School of Pharmacy, Tokyo University of Pharmacy & Life Science , 1432-1 Horinouchi, Hachioji , Tokyo , 192-03 , Japan
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328319608002418
Reference16 articles.
1. The Reaction of O-Benzylidene Sugars with N-Bromosuccinimide.: VI. A New Synthesis of 2′-Deoxyuridine and some of its Selectively Substituted Derivatives
2. The Reaction of O-Benzylidene Sugars with N-Bromosuccinimide.: VII. Stereochemical and Mechanistic Aspects in the Pyrimidine Nucleoside Series
3. NUCLEOSIDES. XIV. SYNTHESIS OF 2'-DEOXY-2'-FLUOROURIDINE1
4. Nucleosides. XVIII. Synthesis of 2'-Fluorothymidine, 2'-Fluorodeoxyuridine, and Other 2'-Halogeno-2'-Deoxy Nucleosides1,2
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1. Independent Generation and Reactivity of Uridin-2′-yl Radical;The Journal of Organic Chemistry;2014-10-17
2. ChemInform Abstract: Partial Protection of Carbohydrate Derivatives. Part 30. Efficient Synthesis of 2′-Bromo-2′-deoxy-3′,5′-O-TPDS-pyrimidine Nucleosides by Boron Trifluoride Catalyzed Reaction of O2,2′-Anhydro-(1-β-D- arabinofuranosyl)pyrimidine Nucleos;ChemInform;2010-08-05
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